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Norrin Mediates Tumor-Promoting and -Suppressive Effects in Glioblastoma Via Notch and Wnt

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Norrin Mediates Tumor-Promoting and -Suppressive Effects in Glioblastoma Via Notch and Wnt The Journal of Clinical Investigation RESEARCH ARTICLE Norrin mediates tumor-promoting and -suppressive effects in glioblastoma via Notch and Wnt Ahmed El-Sehemy,1,2,3 Hayden Selvadurai,4,5 Arturo Ortin-Martinez,1,2,3 Neno Pokrajac,1,2,3 Yasin Mamatjan,6 Nobuhiko Tachibana,1,2,3 Katherine Rowland,4,5 Lilian Lee,4,5 Nicole Park,4,5 Kenneth Aldape,6,7 Peter Dirks,4,5,8,9 and Valerie A. Wallace1,2,3 1Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada. 2Donald K. Johnson Eye Institute, Krembil Research Institute, University Health Network, Toronto, Canada. 3Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Canada. 4Developmental and Stem Cell Biology Program and 5Arthur and Sonia Labatt Brain Tumour Research Centre, Hospital for Sick Children, Toronto, Canada. 6MacFeeters Hamilton Centre for Neuro-Oncology Research, Princess Margaret Cancer Centre, Toronto, Canada. 7Laboratory of Pathology, National Cancer Institute, NIH, Bethesda, Maryland, USA. 8Department of Molecular Genetics, University of Toronto, Toronto, Canada. 9Division of Neurosurgery, Hospital for Sick Children, Toronto, Canada. Glioblastoma multiforme (GBM) contains a subpopulation of cells, GBM stem cells (GSCs), that maintain the bulk tumor and represent a key therapeutic target. Norrin is a Wnt ligand that binds Frizzled class receptor 4 (FZD4) to activate canonical Wnt signaling. Although Norrin, encoded by NDP, has a well-described role in vascular development, its function in human tumorigenesis is largely unexplored. Here, we show that NDP expression is enriched in neurological cancers, including GBM, and its levels positively correlated with survival in a GBM subtype defined by low expression of ASCL1, a proneural factor. We investigated the function of Norrin and FZD4 in GSCs and found that it mediated opposing tumor-suppressive and -promoting effects on ASCL1lo and ASCL1hi GSCs. Consistent with a potential tumor-suppressive effect of Norrin suggested by the tumor outcome data, we found that Norrin signaling through FZD4 inhibited growth in ASCL1lo GSCs. In contrast, in ASCL1hi GSCs Norrin promoted Notch signaling, independently of WNT, to promote tumor progression. Forced ASCL1 expression reversed the tumor-suppressive effects of Norrin in ASCL1lo GSCs. Our results identify Norrin as a modulator of human brain cancer progression and reveal an unanticipated Notch-mediated function of Norrin in regulating cancer stem cell biology. This study identifies an unanticipated role of Norrin in human brain cancer progression. In addition, we provide preclinical evidence suggesting Norrin and canonical Wnt signaling as potential therapeutic targets for GBM subtype–restricted cancer stem cells. Introduction achieve this end, a better understanding of GSC biology is required. Glioblastoma multiforme (GBM) is the most common malignant The Wingless (Wnt) signaling pathway is a major regulator of stem brain cancer in adults (1, 2). Consistent with its progressive nature, cell growth in normal and tumorigenic contexts (19–21) and several GBM remains significantly refractory to current therapeutic strat- Wnt pathway components are reported to regulate GBM progres- egies (3, 4). Temozolomide is the main chemotherapeutic agent sion through effects on GSCs (22). Surprisingly, both inhibition and for the management of GBM; however, it has been shown to be activation of Wnt signaling have been proposed as therapeutic strat- beneficial in a small subset of patients and usually only induces egies in GBM (22–26). Although this discrepancy can be attributed transient effects (5–7). Despite the urgent need for new treatment in part to different culture systems, models, and experimental approaches for GBM, developing such therapies is challenging due conditions used in the different studies, these variable results also to the complex biology of GBM, the difficulty in delivering drugs highlight the complexity of the Wnt pathway and GBM biology. across the blood-brain barrier, and the remarkable heterogeneity Norrin, the protein product of the Norrie disease protein of GBM tumors (8–10). (NDP) gene, is an atypical Wnt ligand that binds the Frizzled class GBMs contain a subpopulation of cells with neural stem cell– receptor 4 (FZD4) and low-density lipoprotein receptor–related like (NSC-like) properties, GBM stem cells (GSCs) (11–14), that can protein 5 (LRP5) receptor complex in the presence of tetraspanin propagate tumors and are thought to be the source of tumor recur- 12 (TSPAN12) to activate canonical (β-catenin–dependent) Wnt rence and treatment resistance (15, 16). Thus, targeting the GSC signaling (27–29). Activation of the Norrin/FZD4 signaling axis in population presents a potentially effective therapeutic approach to endothelial cells has a well-described role in regulating angiogen- overcome the problems facing traditional GBM therapies (17, 18). To esis and blood-brain barrier formation in the cortex, cerebellum, retina, and inner ear (30–33). Paracrine Norrin/FZD4 signaling extends to tumorigenesis, as activation of this pathway in the Related Commentary: p. 2814 endothelium has recently been shown to inhibit medulloblastoma initiation in mice (34). More recently, Norrin has been implicated Conflict of interest: The authors have declared that no conflict of interest exists. in astroglial regulation of neuronal function in the cortex, pointing Copyright: © 2020, American Society for Clinical Investigation. to a role for Norrin beyond the vasculature (35). However, direct Submitted: April 5, 2019; Accepted: March 5, 2020; Published: May 11, 2020. Reference information: J Clin Invest. 2020;130(6):3069–3086. evidence for a functional role for Norrin/FZD4 in human brain https://doi.org/10.1172/JCI128994. tumor progression is lacking. jci.org Volume 130 Number 6 June 2020 3069 RESEARCH ARTICLE The Journal of Clinical Investigation signaling, which is mediated through Notch, to maintain stemness of GSCs. Results NDP expression is enriched in GBM and correlates with survival in neurological cancers. To survey the distribution of NDP expression in human tissues, we queried the human protein atlas (HPA, www.proteinatlas.org) (36), and found that NDP expression, but not that of its receptor FZD4, is enriched in several tissues, including the brain and cerebellum (Supplemental Fig- ure 1A; supplemental material available online with this article; https://doi.org/10.1172/ JCI128994DS1). A similar survey of cancer cell lines (CCLE, https://portals.broadinstitute. org/ccle) (37) and primary tumors (The Can- cer Genome Atlas [TCGA]), shows that NDP is expressed in a variety of tumor types and is highly enriched in glioma cell lines (Supple- mental Figure 1B, boxed) and primary human gliomas, including low-grade glioma (LGG) and GBM (Figure 1A, boxed). In addition, gene set enrichment analysis (GSEA) on GBM showed that NDP expression levels significantly correlate with classical GBM and aging-brain gene sets (Figure 2A). FZD4 is also expressed in different cancer types; however, its expression in GBM is comparable to other cancers (Figure 1B and Supplemental Figure 1, A and B) and not as highly enriched as NDP. The discordance between NDP and FZD4 expression in brain tumors could indicate that NDP, but not FZD4, levels are functionally limiting or that NDP is FZD4 independent. Consistent with the latter possibility, FZD4-independent and nonvas- Figure 1. NDP is expressed in a wide range of cancers, and is enriched in CNS tumors. (A and B) cular functions of NDP have been reported in Analysis of NDP (A) and FZD4 (B) expression levels in primary human tumors from TCGA using the other contexts (38–41). cBioportal web server. NDP expression was significantly enriched in GBM and lower-grade glioma Next, we found that NDP expression cor- relative to the average of all cancer types (upper graph), while FZD4 expression was comparable to relates with survival in GBM, neuroblastoma, other tumor types. ACC, adrenocortical carcinoma; AML, acute myeloid leukemia; DLBC, lymphoid and brain astrocytoma (LGG) (Figure 2B). neoplasm diffuse large B cell lymphoma; PCPG, pheochromocytoma and paraganglioma; CS, carci- nosarcoma; ccRCC, clear cell renal cell carcinoma; chRCC, chromophobe renal cell carcinoma; pRCC, Because transcriptomic data are derived from papillary renal cell carcinoma; VUS, variant of uncertain significance. whole tissue and tumor samples, they do not resolve the cell-type specificity of gene expres- sion, including expression within the tumor In this study, we show that NDP is widely expressed in a range stem cell compartment. Therefore, we analyzed gene expression of neurological and nonneurological cancers, and its expression in hNSCs and primary patient-derived GSCs, which were main- level correlates with patient survival in neurological cancers. Our tained in vitro using an established GSC culture protocol (42). in vitro and in vivo analyses using human fetal NSCs (hNSCs) and Quantitative real-time PCR (qRT-PCR) revealed that NDP, FZD4, primary patient-derived GSCs reveals an endothelial cell–inde- LRP5, and TSPAN12 are expressed in hNSCs and in the majority pendent role for NDP in regulating GSC proliferation, cell cycle of the GSC lines we surveyed (Figure 2C). The enrichment of NDP progression, and tumorigenicity. Interestingly, our data show that expression in brain tumors, expression of Norrin/FZD4 signaling NDP function and the growth-modulatory effects of canoni- components in primary GSCs, and the association
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